Coagulation factor VII
Also known as: F7
Function
Initiates the extrinsic pathway of blood coagulation. Serine protease that circulates in the blood in a zymogen form. Factor VII is converted to factor VIIa by factor Xa, factor XIIa, factor IXa, or thrombin by minor proteolysis. In the presence of tissue factor and calcium ions, factor VIIa then converts factor X to factor Xa by limited proteolysis. Factor VIIa also converts factor IX to factor IXa in the presence of tissue factor and calcium.
Classification
- Family (Pfam)
- PF00008 EGF, PF14670 FXa_inhibition, PF00594 Gla, PF00089 Trypsin
- InterPro
- Coagulation_fac-like_Gla_dom, EGF, EGF-like_Ca-bd_dom, EGF-type_Asp/Asn_hydroxyl_site, EGF_Ca-bd_CS, GLA-like_dom_SF, GLA_domain, Pept_S1A_FX, Peptidase_S1_coag_factors, Peptidase_S1_PA, Peptidase_S1_PA_chymotrypsin, Peptidase_S1A, Trypsin_dom, TRYPSIN_HIS, TRYPSIN_SER
- Functional cluster
- Venom Serine Proteases & Phospholipase A2
Experimental structures · PDB · 113
- 1BF9 NMR
- 1CVW X-ray 2.28A
- 1DAN X-ray 2.00A
- 1DVA X-ray 3.00A
- 1F7E NMR
- 1F7M NMR
- 1FAK X-ray 2.10A
- 1FF7 NMR
- 1FFM NMR
- 1J9C X-ray 2.90A
- 1JBU X-ray 2.00A
- 1KLI X-ray 1.69A
- … and 101 more
A predicted model is available from AlphaFold.
Gene Ontology · 35
- GO:0005788 endoplasmic reticulum lumen
- GO:0031012 extracellular matrix
- GO:0005576 extracellular region
- GO:0005615 extracellular space
- GO:0005796 Golgi lumen
- GO:0005886 plasma membrane
- GO:1905286 serine-type peptidase complex
- GO:0031982 vesicle
- GO:0005509 calcium ion binding
- GO:0004252 serine-type endopeptidase activity
- GO:0008236 serine-type peptidase activity
- GO:0005102 signaling receptor binding
- GO:0031100 animal organ regeneration
- GO:0007596 blood coagulation
- GO:0007623 circadian rhythm
- GO:0030194 positive regulation of blood coagulation
- GO:0030335 positive regulation of cell migration
- GO:0002690 positive regulation of leukocyte chemotaxis
- GO:0010641 positive regulation of platelet-derived growth factor receptor signaling pathway
- GO:0050927 positive regulation of positive chemotaxis
- GO:0032008 positive regulation of TOR signaling
- GO:0016485 protein processing
- GO:1904612 response to 2,3,7,8-tetrachlorodibenzodioxine
- GO:1905217 response to astaxanthin
- GO:0010037 response to carbon dioxide
- GO:0070723 response to cholesterol
- GO:0032355 response to estradiol
- GO:0043627 response to estrogen
- GO:0033595 response to genistein
- GO:0060416 response to growth hormone
- GO:0001666 response to hypoxia
- GO:1904400 response to Thyroid stimulating hormone
- GO:1905225 response to thyrotropin-releasing hormone
- GO:0097068 response to thyroxine
- GO:0032571 response to vitamin K
Disease associations
- congenital factor VII deficiency MONDO:0009211
Drugs targeting this protein · 1
- PCI-27483 inhibitor
Related proteins · sequence + function similarity
- Coagulation factor VII 1.00
- Coagulation factor VII 1.00
- Coagulation factor VII 0.97
- Coagulation factor VII 0.97
- Vitamin K-dependent protein C 0.97
- Vitamin K-dependent protein C 0.96
- Vitamin K-dependent protein C 0.96
- Vitamin K-dependent protein C 0.96
- Vitamin K-dependent protein C 0.96
- Coagulation factor VII 0.96
- Vitamin K-dependent protein C 0.95
- Vitamin K-dependent protein C 0.94
Co-cited proteins · studied together in the literature
- Tissue factor 3 shared papers
- Coagulation factor VII 1 shared papers
- Coagulation factor VII 1 shared papers
- Coagulation factor IX 4 shared papers
- Vitamin K-dependent protein Z 2 shared papers
- GDP-fucose protein O-fucosyltransferase 1 1 shared papers
- Vitamin K-dependent protein Z 2 shared papers
- GDP-fucose protein O-fucosyltransferase 1 1 shared papers
- Protein O-glucosyltransferase 1 1 shared papers
- Dipeptidyl peptidase 1 1 shared papers
- Protein O-glucosyltransferase 1 1 shared papers
- Coagulation factor VII 1 shared papers
Literature · 48 cited papers
- Structural and functional characterization of novel F7 mutations identified in Chinese factor VII-deficient patients. Br. J. Haematol. · 2023
- Ixodes ricinus Salivary Serpin Iripin-8 Inhibits the Intrinsic Pathway of Coagulation and Complement. Int. J. Mol. Sci. · 2021
- Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s. Blood Coagul. Fibrinolysis · 2016
- Rumi functions as both a protein O-glucosyltransferase and a protein O-xylosyltransferase. Proc. Natl. Acad. Sci. U.S.A. · 2011
- A novel missense mutation close to the charge-stabilizing system in a patient with congenital factor VII deficiency. Blood Coagul. Fibrinolysis · 2011
- Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea. Blood Coagul. Fibrinolysis · 2011
- Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India. Clin. Chim. Acta · 2009
- Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation. Haemophilia · 2009
- Cotranslational and posttranslational N-glycosylation of polypeptides by distinct mammalian OST isoforms. Cell · 2009
- Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene. Haemophilia · 2009
- Human F7 sequence is split into three deep clades that are related to FVII plasma levels. Hum. Genet. · 2006
- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. · 2004
- … and 36 more in the literature graph
A document in the lmmol reference corpus — open public data (UniProt, GO, PDB, the literature graph) rendered as a single cross-linked page. Hover any link to preview its target.